Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Aminopyridine-2-sulfonamide | HCID 14943702 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-Fluoropyridine-2-sulfonamide | HCID 19957930 | 70% |
Reaction Steps
5.3 g (0.030 mol) of 3-aminopyridin-2-ylsulfonamide are dissolved in 12 ml of dimethyl sulfoxide, and the solution is added dropwise at 0° C. to 14.3 g (0.72 mol) of hydrogen fluoride (exothermal reaction). 2.4 g (0.035 mol) of sodium nitrite are then added in portions at 0° C. After one hour, the mixture is heated to 70° C. (evolution of N2). After the reaction mixture has cooled, it is added to an ice/water mixture, sodium bicarbonate and sodium chloride are added, and the mixture is then extracted with tetrahydrofuran and ethyl acetate. The combined extracts are washed with a saturated sodium chloride solution, dried with magnesium sulfate, filtered and evaporated. The residue is stirred in diethyl ether/petroleum ether. Filtration gives 3.7 g of 3-fluoropyridin-2-ylsulfonamide (Compound No. 3.001) of a melting point of +124° to +125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05410063 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-429577d82d2a4a40b7f728b09be5c3bf |
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| Source note | uspto-grants-1995_04 |
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